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A Pilot Study of the Use of the DaVinci Robotic System for Otorhinolaryngology-Head and Neck Surgery

A Pilot Study of the Use of the DaVinci Robotic System for Otorhinolaryngology-Head and Neck Surgery

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00627562
Enrollment
71
Registered
2008-03-03
Start date
2007-07-31
Completion date
2017-12-31
Last updated
2016-03-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Head and Neck Neoplasms

Keywords

robotic, robot assisted, minimally invasive, tumors of head and neck

Brief summary

1. Patients included will have benign or malignant lesions with treatment plan for endoscopic resection or resection by other minimally invasive techniques. 2. They will be offered a robotic approach to their surgery using the DaVinci robotic surgical system (intuitive Surgical, Inc.). 3. The objectives are to evaluate our ability to adequately visualize the surgical field and perform the intended surgery without a higher complication rate. 4. Secondary objective include evaluation of blood loss, length of hospital stay, complications while using the DaVinci robot system, and quality of life in subjects and historical controls undergoing similar surgery without the robot or radiation therapy. 5. To evaluate recurrence, survival and other outcome data in robotic surgery patients compared with similar historical control groups (matched with respect to stage, prior and subsequent treatment, age, tumor HPV positivity) of patients who have undergone standard surgery without the robot or radiation/chemoradiation treatment as an alternative to surgery. 5\. Endpoints will be compared to historical controls.

Detailed description

The da Vinci® Robotic Surgical System (Intuitive Surgical, Inc., Sunnyvale, CA) being evaluated in this pilot study consists of 3 basic components: a surgeon's console, articulated mechanical arms and sterilizable instruments. The console includes a computer, video monitor and instrument controls, and is located in the operating room adjacent to the operating room table. The console is connected via computer to the mechanical arms holding the endoscope (surgical TV camera) and sterile surgical tools (e.g., forceps, scissors, electrocautery, etc.). These arms are located immediately adjacent to the patient on the operating room table. The surgeon sits at the console and controls the position and movement of the arms and surgical tools. The design of these tools is based upon well-established, commonly used surgical instruments. The da Vinci® Robotic Surgical System (Intuitive Surgical, Inc., Sunnyvale, CA) is a manual image-guided surgery system that is computer enhanced rather than computer guided robotic surgery in which the surgeon programs the computer to do the surgery and the robot does the surgery (also known as a milling device).22 Use of the da Vinci® Robotic Surgical System (Intuitive Surgical, Inc., Sunnyvale, CA) in the aforementioned configuration in fact facilitates an exact translation of the surgeon's hand and finger movements at the console to precise and tremor-free movements of the arms and instruments.

Interventions

DEVICErobot assisted endoscopic head and neck surgery using the DaVinci Robotic Surgical System

Planned endoscopic surgery of the head and neck performed with the DaVinci Robotic Surgical System

Sponsors

Montefiore Medical Center
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* At least 18 years f age * Indications for diagnostic or therapeutic approaches for benign or malignant disease of the head and neck * Written informed consent

Exclusion criteria

* Unexplained fever and/or untreated, active infection * Pregnancy * Previous head and neck surgery precluding transoral/endoscopic/robotic procedures * Presence of medical conditions contraindicating general anesthesia or transoral surgical approaches

Design outcomes

Primary

MeasureTime frame
ability to adequately visualize the operative field and complete planned surgery1 day

Secondary

MeasureTime frame
blood loss compared to historical controls of endoscopic and minimally invasive procedures1 day
quality of life at early (1-3 months) and late (one year)1 year
complication rate compared to standard endoscopic and minimally invasive procedures1 month
Time to recurrence of tumor or other pathology for which procedure was performedat recurrence of tumor or pathology
Time from start of treatment to deathat time of death
number of days hospitalized immediately after surgeryat discharge from hospital

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026